Welcome to the UPF Digital Repository

A glutamine-based single α-helix scaffold to target globular proteins

Show simple item record

dc.contributor.author Escobedo, Albert
dc.contributor.author Piccirillo, Jonathan
dc.contributor.author Aranda, Juan
dc.contributor.author Diercks, Tammo
dc.contributor.author Mateos, Borja
dc.contributor.author Garcia-Cabau, Carla
dc.contributor.author Sánchez-Navarro, Macarena
dc.contributor.author Topal, Busra
dc.contributor.author Biesaga, Mateusz
dc.contributor.author Staby, Lasse
dc.contributor.author Kragelund, Birthe B.
dc.contributor.author García, Jesús
dc.contributor.author Millet, Oscar
dc.contributor.author Orozco, Modesto
dc.contributor.author Coles, Murray
dc.contributor.author Crehuet, Ramon
dc.contributor.author Salvatella, Xavier
dc.date.accessioned 2023-01-24T07:19:36Z
dc.date.available 2023-01-24T07:19:36Z
dc.date.issued 2022
dc.identifier.citation Escobedo A, Piccirillo J, Aranda J, Diercks T, Mateos B, Garcia-Cabau C, Sánchez-Navarro M, Topal B, Biesaga M, Staby L, Kragelund BB, García J, Millet O, Orozco M, Coles M, Crehuet R, Salvatella X. A glutamine-based single α-helix scaffold to target globular proteins. Nat Commun. 2022 Nov 18;13(1):7073. DOI: 10.1038/s41467-022-34793-6
dc.identifier.issn 2041-1723
dc.identifier.uri http://hdl.handle.net/10230/55410
dc.description.abstract The binding of intrinsically disordered proteins to globular ones can require the folding of motifs into α-helices. These interactions offer opportunities for therapeutic intervention but their modulation with small molecules is challenging because they bury large surfaces. Linear peptides that display the residues that are key for binding can be targeted to globular proteins when they form stable helices, which in most cases requires their chemical modification. Here we present rules to design peptides that fold into single α-helices by instead concatenating glutamine side chain to main chain hydrogen bonds recently discovered in polyglutamine helices. The resulting peptides are uncharged, contain only natural amino acids, and their sequences can be optimized to interact with specific targets. Our results provide design rules to obtain single α-helices for a wide range of applications in protein engineering and drug design.
dc.description.sponsorship We thank Luis Serrano for help with the Agadir predictions and helpful discussions, Ben Lehner and Ernest Giralt for helpful discussions and the ICTS NMR facility, managed by the scientific and technological centers of the University of Barcelona (CCiT UB), for their help in NMR. B.M. acknowledges funding from the Asociación Española contra el Cáncer (FCAECC project #POSTD211371MATE). C.G. acknowledges a graduate fellowship from MINECO (PRE2018-084684). M.S.-N. acknowledges funding from MINECO (PID2020-119810RB-I00). M.S.-N. holds a Ramón y Cajal contract (RYC2018-024759-I) from the Spanish Ministry of Science, Innovation, and Universities. X.S. acknowledges funding from AGAUR (2017 SGR 324), MINECO (BIO2015-70092-R and PID2019-110198RB-I00), and the European Research Council (CONCERT, contract number 648201). B.B.K acknowledges funding from the Novo Nordisk Foundation (#NNF18OC0033926). M.O. acknowledges funding from the Instituto Nacional de Bioinformática, The EU BioExcel Centre of Excellence for HPC and the Spanish Ministry of Science (PID2021-122478NB-I00) and the Instituto de Salud Carlos III–Instituto Nacional de Bioinformatica (ISCIII PT 17/0009/0007 co-funded by the Fondo Europeo de Desarrollo Regional). M.O. is an ICREA Academy scholar and J.A. is a Juan de la Cierva fellow. M.C. was supported by institutional funds of the Max Planck Society. This project has been carried out using the resources of CSUC. IRB Barcelona is the recipient of a Severo Ochoa Award of Excellence from MINECO (Government of Spain).
dc.format.mimetype application/pdf
dc.language.iso eng
dc.publisher Nature Research
dc.relation.ispartof Nat Commun. 2022 Nov 18;13(1):7073
dc.rights © The Author(s) 2022. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
dc.rights.uri http://creativecommons.org/licenses/by/4.0/
dc.title A glutamine-based single α-helix scaffold to target globular proteins
dc.type info:eu-repo/semantics/article
dc.identifier.doi http://dx.doi.org/10.1038/s41467-022-34793-6
dc.subject.keyword Biophysical chemistry
dc.subject.keyword Intrinsically disordered proteins
dc.subject.keyword Peptides
dc.subject.keyword Solution-state NMR
dc.relation.projectID info:eu-repo/grantAgreement/EC/H2020/648201
dc.relation.projectID info:eu-repo/grantAgreement/ES/2PE/PRE2018-084684
dc.relation.projectID info:eu-repo/grantAgreement/ES/2PE/PID2020-119810RB-I00
dc.relation.projectID info:eu-repo/grantAgreement/ES/1PE/BIO2015-70092-R
dc.relation.projectID info:eu-repo/grantAgreement/ES/2PE/PID2019-110198RB-I00
dc.relation.projectID info:eu-repo/grantAgreement/ES/3PE/PID2021-122478NB-I00
dc.rights.accessRights info:eu-repo/semantics/openAccess
dc.type.version info:eu-repo/semantics/publishedVersion


This item appears in the following Collection(s)

Show simple item record

Search DSpace

Advanced Search


My Account


In collaboration with Compliant to Partaking